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4. Homogentisic acid oxidase activity in homozygous and heterozygous alkaptonuric mice. Coudé M; Montagutelli X; Guenet JL; Kamoun P Ann Biol Clin (Paris); 1994; 52(7-8):569-70. PubMed ID: 7840434 [No Abstract] [Full Text] [Related]
5. Exacerbation of the ochronosis of alkaptonuria due to renal insufficiency and improvement after renal transplantation. Introne WJ; Phornphutkul C; Bernardini I; McLaughlin K; Fitzpatrick D; Gahl WA Mol Genet Metab; 2002; 77(1-2):136-42. PubMed ID: 12359141 [TBL] [Abstract][Full Text] [Related]
6. Purification of the homogentisic acid oxidase from mammalian liver. Hudecová S; Straková Z; Krizanova O Int J Biochem Cell Biol; 1995 Dec; 27(12):1357-63. PubMed ID: 8581831 [No Abstract] [Full Text] [Related]
7. Evaluation of antioxidant drugs for the treatment of ochronotic alkaptonuria in an in vitro human cell model. Tinti L; Spreafico A; Braconi D; Millucci L; Bernardini G; Chellini F; Cavallo G; Selvi E; Galeazzi M; Marcolongo R; Gallagher JA; Santucci A J Cell Physiol; 2010 Oct; 225(1):84-91. PubMed ID: 20648626 [TBL] [Abstract][Full Text] [Related]
8. aku, a mutation of the mouse homologous to human alkaptonuria, maps to chromosome 16. Montagutelli X; Lalouette A; Coudé M; Kamoun P; Forest M; Guénet JL Genomics; 1994 Jan; 19(1):9-11. PubMed ID: 8188247 [TBL] [Abstract][Full Text] [Related]
9. Alkaptonuria presenting with ochronotic spondyloarthropathy. Al-Mahfoudh R; Clark S; Buxton N Br J Neurosurg; 2008 Dec; 22(6):805-7. PubMed ID: 19085367 [TBL] [Abstract][Full Text] [Related]
10. Evaluation of anti-oxidant treatments in an in vitro model of alkaptonuric ochronosis. Braconi D; Laschi M; Amato L; Bernardini G; Millucci L; Marcolongo R; Cavallo G; Spreafico A; Santucci A Rheumatology (Oxford); 2010 Oct; 49(10):1975-83. PubMed ID: 20601653 [TBL] [Abstract][Full Text] [Related]
11. Conditional targeting in mice reveals that hepatic homogentisate 1,2-dioxygenase activity is essential in reducing circulating homogentisic acid and for effective therapy in the genetic disease alkaptonuria. Hughes JH; Liu K; Plagge A; Wilson PJM; Sutherland H; Norman BP; Hughes AT; Keenan CM; Milan AM; Sakai T; Ranganath LR; Gallagher JA; Bou-Gharios G Hum Mol Genet; 2019 Dec; 28(23):3928-3939. PubMed ID: 31600782 [TBL] [Abstract][Full Text] [Related]
12. [Diagnostic image (45). Ochronosis]. ter Borg EJ Ned Tijdschr Geneeskd; 2001 Jul; 145(27):1295. PubMed ID: 11475020 [TBL] [Abstract][Full Text] [Related]
13. [Ochronosis: a case report with multisystemic affectation, including pericardium]. Cobos Soler FJ; Molero Cabrilla R An Med Interna; 2002 Nov; 19(11):583-5. PubMed ID: 12522896 [TBL] [Abstract][Full Text] [Related]
14. Alkaptonuria in a 5-year-old boy in Iraq. Al-Mefraji SH East Mediterr Health J; 2008; 14(3):745-6. PubMed ID: 18720640 [No Abstract] [Full Text] [Related]
15. Effects of ascorbic acid in alkaptonuria: alterations in benzoquinone acetic acid and an ontogenic effect in infancy. Wolff JA; Barshop B; Nyhan WL; Leslie J; Seegmiller JE; Gruber H; Garst M; Winter S; Michals K; Matalon R Pediatr Res; 1989 Aug; 26(2):140-4. PubMed ID: 2771520 [TBL] [Abstract][Full Text] [Related]
16. A novel therapeutic trial of homogentisic aciduria in a murine model of alkaptonuria. Suzuki Y; Oda K; Yoshikawa Y; Maeda Y; Suzuki T J Hum Genet; 1999; 44(2):79-84. PubMed ID: 10083729 [TBL] [Abstract][Full Text] [Related]
17. Spectrophotometric determination of homogentisate using Aspergillus nidulans homogentisate dioxygenase. Fernández-Cañón JM; Peñalva MA Anal Biochem; 1997 Feb; 245(2):218-21. PubMed ID: 9056215 [TBL] [Abstract][Full Text] [Related]
18. Alkaptonuria: such a long journey. Scriver CR Nat Genet; 1996 Sep; 14(1):5-6. PubMed ID: 8782808 [No Abstract] [Full Text] [Related]
19. Monitoring of a one-month ascorbic acid therapy in an alcaptonuric child; determinations by HPLC. Simoni RE; Gomes LN; Faria MS; Barbara Neto J; de Oliveira ML J Inherit Metab Dis; 1994; 17(5):632-3. PubMed ID: 7837775 [No Abstract] [Full Text] [Related]
20. Sequence analysis of the homogentisate 1,2 dioxygenase gene in a family affected by alkaptonuria. Walter K; Gaa A; Schaefer HE J Med Genet; 1999 Aug; 36(8):645-6. PubMed ID: 10465119 [No Abstract] [Full Text] [Related] [Next] [New Search]